Instagram
youtube
Facebook
2+ years
Not Disclosed
10 Oct. 7, 2024
Job Description
Job Type: Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Description

About Thermo Fisher Scientific Inc.

Thermo Fisher Scientific Inc. is a global leader in the life sciences sector, delivering top-notch solutions to pharmaceutical companies, biotech firms, and Clinical Research Organizations (CROs). As a trusted partner to some of the most innovative companies in the industry, we offer exciting opportunities for experienced Safety Writers to work on diverse projects across a wide array of therapeutic areas.

Position Overview

As a Safety Writer at Thermo Fisher Scientific, you will play a vital role in delivering high-quality scientific and medical writing services. You'll be an integral part of project teams, providing exceptional customer service and collaborating with clients to ensure successful project execution. Your key responsibilities will include:

  • Analyzing, interpreting, and presenting complex data effectively.
  • Writing clear and concise reports and documents.
  • Managing multiple reports simultaneously while prioritizing tasks to meet strict deadlines.
  • Facilitating meetings and overseeing the review and comment resolution stages of document preparation.
  • Interacting directly with clients to provide outstanding customer service.

Qualifications

To qualify for this position, you must have:

  • A Bachelor’s or higher degree in a scientific field.
  • Excellent written and verbal communication skills in English.
  • Advanced proficiency in Microsoft Office applications.
  • Experience in task-based project management and client interaction.
  • A strong understanding of aggregate safety report writing guidelines, as well as clinical trial and post-marketing pharmacovigilance.
  • Preferably, experience in authoring device aggregate safety reports or clinical evaluation reports.

Additionally, you should have a minimum of two years’ experience in authoring at least two of the following report/document types for medicinal products:

  • Development Safety Update Reports (DSURs)
  • Periodic Benefit Risk Evaluation Reports (PBRERs) / Periodic Safety Update Reports (PSURs)
  • Periodic Adverse Drug Experience Reports (PA(D)ERs)
  • Risk Management Plans (RMPs)

Our Offer

At Thermo Fisher Scientific, we foster a positive and supportive working environment within one of the most engaged teams in the industry. We recognize that our employees are the cornerstone of our success and provide ample opportunities for personal and professional growth. We also offer a competitive remuneration package and corporate training programs.

To apply for this position, please submit your CV in English through our website.

Please note that only shortlisted candidates will be contacted.

Thermo Fisher Scientific is an equal opportunity employer.